RS200386310 SPTB

Health Risk Chr 14:64772678
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What This Variant Does
"CLNSIG=4
Associated Conditions
Hereditary spherocytosis type 2
Hereditary spherocytosis type 2
Other Variants in SPTB
rs121918645 rs863223302 rs863223303 rs1594753904 rs121918646 rs121918647 rs121918648 rs121918649 rs121918650 rs121918651
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